tert-butyl 4-[N-(2-methyl-3-(2,2-dimethylpropionyloxymethyl)-4-oxo-3,4,7,8-tetrahydro-6H-cyclopenta[g]quinazolin-6-yl)-N-(prop-2-ynyl)amino]benzoate

Base Information

Chemical Name:tert-butyl 4-[N-(2-methyl-3-(2,2-dimethylpropionyloxymethyl)-4-oxo-3,4,7,8-tetrahydro-6H-cyclopenta[g]quinazolin-6-yl)-N-(prop-2-ynyl)amino]benzoate
CAS No.:902777-37-1
Molecular Formula:C₃₂H₃₇N₃O₅
Molecular Weight:543.663
Hs Code.:

tert-butyl 4-[N-(2-methyl-3-(2,2-dimethylpropionyloxymethyl)-4-oxo-3,4,7,8-tetrahydro-6H-cyclopenta[g]quinazolin-6-yl)-N-(prop-2-ynyl)amino]benzoate

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Chemical Property of tert-butyl 4-[N-(2-methyl-3-(2,2-dimethylpropionyloxymethyl)-4-oxo-3,4,7,8-tetrahydro-6H-cyclopenta[g]quinazolin-6-yl)-N-(prop-2-ynyl)amino]benzoate

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Technology Process of tert-butyl 4-[N-(2-methyl-3-(2,2-dimethylpropionyloxymethyl)-4-oxo-3,4,7,8-tetrahydro-6H-cyclopenta[g]quinazolin-6-yl)-N-(prop-2-ynyl)amino]benzoate

There total 3 articles about tert-butyl 4-[N-(2-methyl-3-(2,2-dimethylpropionyloxymethyl)-4-oxo-3,4,7,8-tetrahydro-6H-cyclopenta[g]quinazolin-6-yl)-N-(prop-2-ynyl)amino]benzoate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 157701-46-7
tert-butyl 4-[N-(2-methyl-3-(2,2-dimethylpropionyloxymethyl)-4-oxo-3,4,7,8-tetrahydro-6H-cyclopenta[g]quinazolin-6-yl)amino]benzoate

: 902777-37-1
tert-butyl 4-[N-(2-methyl-3-(2,2-dimethylpropionyloxymethyl)-4-oxo-3,4,7,8-tetrahydro-6H-cyclopenta[g]quinazolin-6-yl)-N-(prop-2-ynyl)amino]benzoate

Guidance literature:: tert-butyl 4-[N-(2-methyl-3-(2,2-dimethylpropionyloxymethyl)-4-oxo-3,4,7,8-tetrahydro-6H-cyclopenta[g]quinazolin-6-yl)amino]benzoate; (propargyl)Co₂(CO)6⁽¹⁺⁾*BF₄^(1-); With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃; for 1h;

With ferric nitrate; In ethanol; at 20 ℃; for 1h;
DOI:10.1016/j.bmc.2006.03.001

Reference yield:

: 18144-47-3
tert-butyl 4-aminobenzoate

: 902777-37-1
tert-butyl 4-[N-(2-methyl-3-(2,2-dimethylpropionyloxymethyl)-4-oxo-3,4,7,8-tetrahydro-6H-cyclopenta[g]quinazolin-6-yl)-N-(prop-2-ynyl)amino]benzoate

Guidance literature:: Multi-step reaction with 2 steps

1.1: 46 percent / decaborane / methanol; acetonitrile / 18 h / 20 °C

2.1: ethyldiisopropylamine / CH₂Cl₂ / 1 h / 20 °C

2.2: Fe(NO₃)3*9H₂O / ethanol / 1 h / 20 °C

With Decaborane; N-ethyl-N,N-diisopropylamine; In methanol; dichloromethane; acetonitrile;
DOI:10.1016/j.bmc.2006.03.001

Reference yield:

: 174487-97-9
2-methyl-3-(2,2-dimethylpropionyloxymethyl)-3,4,7,8-tetrahydro-6H-cyclopenta[g]quinazoline-4,6-dione

: 902777-37-1
tert-butyl 4-[N-(2-methyl-3-(2,2-dimethylpropionyloxymethyl)-4-oxo-3,4,7,8-tetrahydro-6H-cyclopenta[g]quinazolin-6-yl)-N-(prop-2-ynyl)amino]benzoate

Guidance literature:: Multi-step reaction with 2 steps

1.1: 46 percent / decaborane / methanol; acetonitrile / 18 h / 20 °C

2.1: ethyldiisopropylamine / CH₂Cl₂ / 1 h / 20 °C

2.2: Fe(NO₃)3*9H₂O / ethanol / 1 h / 20 °C

With Decaborane; N-ethyl-N,N-diisopropylamine; In methanol; dichloromethane; acetonitrile;
DOI:10.1016/j.bmc.2006.03.001